Canonical Allele Identifier: CA2813847009

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785159_18785160del , CM000681.2:g.18785159_18785160del	GRCh38
NC_000019.9:g.18895969_18895970del , CM000681.1:g.18895969_18895970del	GRCh37
NC_000019.8:g.18756969_18756970del	NCBI36
NG_007070.1:g.11146_11147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1718-67_1718-66del MANE Select	ENSP00000222271.2:n.1718-67_1718-66del
ENST00000222271.6:c.1718-67_1718-66del	ENSP00000222271.2:n.1718-67_1718-66del
ENST00000425807.1:c.1559-67_1559-66del	ENSP00000403792.1:n.1559-67_1559-66del
ENST00000542601.6:c.1619-67_1619-66del	ENSP00000439156.2:n.1619-67_1619-66del
NM_000095.2:c.1718-67_1718-66del	NP_000086.2:n.1718-67_1718-66del
NM_000095.3:c.1718-67_1718-66del MANE Select	NP_000086.2:n.1718-67_1718-66del